Large-scale DFT simulation of quinone molecules encapsulated in single-walled carbon nanotube for novel Li-ion battery cathode

Abstract

A system of quinone molecules encapsulated in single-walled carbon nanotubes (SWCNTs) has been proposed as a next-generation cathode material for rechargeable batteries [Y. Ishii et al., Phys. Chem. Chem. Phys. 18 (2016) 10411–10418]. We use density functional theory (DFT) to theoretically investigate (i) the electronic and structural states of SWCNT-encapsulated quinone with or without Li and (ii) the Li insertion and extraction dynamics in the system. Substantial electron transfer from the quinone molecules to the SWCNT is thereby observed. This electron transfer stabilizes the positively charged quinone molecules in the negatively charged SWCNT through Coulomb attraction and decreases the electronic band gap for the SWCNT with semiconductor chirality. In the case of 9,10-phenanthrenequinone (PhQ), we observe that the cross-sectional shape of the SWCNT changes substantially in the relaxed state depending on the extent of Li insertion: the SWCNT exhibits a circular cylinder shape when no Li is present, whereas it is flattened upon sufficient Li insertion. These SWCNT shapes well reflect the aggregated shapes of PhQ molecules, which depend on the amount of Li inserted. As for the Li insertion and extraction dynamics, we find that the Li atoms can take either of two paths: one is along the SWCNT wall, and the other involves hopping on the PhQ molecules and/or the sites where the C atoms of the SWCNT and the O atoms of PhQ molecules contact each other. The Li-transfer rate on the SWCNT wall is large; hence, the hopping is the rate-limiting step.